# Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.

- Location (FDA's records): Ljubljana, SI
- FDA decisions: 2 (2022–2023): 2 510(k) clearances
- Product codes: DPS (1), JOM (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cardioline S.P.A: 1 (https://510kreport.com/company/cardioline)

## Recent decisions
- K223670: MESI mTablet ECG Diagnostic System, MESI mTablet ECG (Jul 28, 2023)
- K213730: MESI mTABLET TBI diagnostic system, MESI mTABLET TBI (Apr 21, 2022)

Source page: https://510kreport.com/company/mesi-development-of-medical-devices-mesi-doo